# Chlordiazepoxide Hydrochloride

NDC: 87441-015
Generic name: Chlordiazepoxide Hydrochloride
Labeler / Manufacturer: Unit Dose Solutions, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20260608

FDA application: ANDA084769

## Active ingredients

- CHLORDIAZEPOXIDE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"87441-015"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=87441-015
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=53c278b6-d22d-79bd-e063-6294a90a82cd